The recurrence risks for isolated cases with incompletely penetrant X-linked conditions
- Author
- ROGATKO, A1
[1] Memorial Sloan-Kettering cancer cent., New York NY 10021, United States - Source
Genetic epidemiology. 1986, Vol 3, Num 5, pp 357-364 ; ref : 4 ref
- Publisher
- Wiley-Liss, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alport syndrome Caractère lié au sexe Chromosome X Conseil génétique Fragilité chromosomique Génétique épidémiologique Homme Maladie Pénétrance génique Rein pathologie Surdité Syndrome complexe Syndrome X fragile
- Keyword (en)
- Alport syndrome Sex linked character X-Chromosome Genetic counseling Chromosome fragility Epidemiologic genetics Fragile X syndrome Human Disease Gene penetrance Renal disease Hearing loss Complex syndrome
- Keyword (es)
- Alport sindrome Caracter ligado al sexo Cromosoma X Consejo genetico Fragilidad cromosómica Hombre Enfermedad Penetrancia genica Riñon patologia Sordera Síndrome complejo
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8216070
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/gepi.1370030508 
https://dx.doi.org/10.1002/gepi.1370030508
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